Document Detail

Newer treatments for decompensated heart failure: focus on levosimendan.
Jump to Full Text
MedLine Citation:
PMID:  19920923     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Acute heart failure (AHF) is a major cause of hospitalizations. Severe dyspnea, pulmonary congestion and low cardiac output with peripheral vasoconstriction and renal hypoperfusion is a main form of clinical presentation. Most patients with acute worsening have a pre-existing decompensated chronic heart failure (ADCHF), but AHF may also occur as a first manifestation of a previously unknown heart disease. Myocardial ischemia, cardiac arrhythmias, non-compliance with medication and infections are frequent precipitating factors. Management of AHF depends on the underlying heart disease and cause of decompensation. In patients with ADCHF vasodilators and iv diuretics are first-line drugs for rapid reduction of dyspnea and congestion. In patients with signs of low cardiac output and oliguria, inotropic agents are also often administered to prevent further deterioration. Beta-adrenergic agents and phosphodiesterase inhibitors correct the hemodynamic disturbance, but may also induce arrhythmias and worsen myocardial ischemia. Inotropic therapy therefore remains controversial. A novel class of drugs, the calcium sensitizers, represent a new therapeutic option. Levosimendan was shown to improve myocardial contractility without increasing oxygen requirements and to produce peripheral and coronary vasodilation. Its therapeutic effects and tolerance have been tested in several trials. The present review focuses on the clinical pharmacology and therapeutic utility of levosimendan in patients with ADCHF.
Authors:
Ferenc Follath
Related Documents :
25430403 - Predictors of successful percutaneous transvenous mitral commissurotomy using the bonho...
25194953 - Long-term clinical outcomes after sirolimus-eluting stent implantation for unprotected ...
15653013 - Cardiac medical therapy in patients after undergoing coronary artery bypass graft surge...
Publication Detail:
Type:  Journal Article     Date:  2009-09-21
Journal Detail:
Title:  Drug design, development and therapy     Volume:  3     ISSN:  1177-8881     ISO Abbreviation:  Drug Des Devel Ther     Publication Date:  2009  
Date Detail:
Created Date:  2009-11-20     Completed Date:  2012-09-10     Revised Date:  2013-05-23    
Medline Journal Info:
Nlm Unique ID:  101475745     Medline TA:  Drug Des Devel Ther     Country:  New Zealand    
Other Details:
Languages:  eng     Pagination:  73-8     Citation Subset:  -    
Affiliation:
Steering Group Drug Therapy, University Hospital Zürich, Raemistrasse 100, Zürich, Switzerland. ferenc.follath@usz.ch
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Full Text
Journal Information
Journal ID (nlm-ta): Drug Des Devel Ther
Journal ID (publisher-id): Drug Design, Development and Therapy
ISSN: 1177-8881
Publisher: Dove Medical Press
Article Information
Download PDF
? 2009 Follath, publisher and licensee Dove Medical Press Ltd.
License:
collection publication date: Year: 2009
Electronic publication date: Day: 21 Month: 9 Year: 2009
Volume: 3First Page: 73 Last Page: 78
ID: 2769227
PubMed Id: 19920923
Publisher Id: dddt-3-073

Newer treatments for decompensated heart failure: focus on levosimendan
Ferenc Follath
University Hospital Z?rich, Steering, Group Drug Therapy, Z?rich, Switzerland
Correspondence: Correspondence: Ferenc Follath, University Hospital Z?rich, Office HAL, 18/D2, Raemistr. 100, CH 8091 Z?rich, Switzerland, Tel +41 44 255 9305, Fax +41 44 255 4554, Email ferenc.follath@usz.ch

Introduction

Therapeutic guidelines have been primarily developed for patients with chronic heart failure (CHF). Recommendations are based on large scale trials with angiotensin-converting enzyme (ACE) inhibitors, angiotensin receptor antagonists and beta-blockers conducted in symptomatic patients with reduced left ventricular ejection fraction, usually <35% to 40%, in a stable phase. More recently, attention also turned to acute and worsening heart failure which is a major cause of hospitalizations. Several epidemiological surveys in Europe1?4 and in the USA5 described the demographics, symptoms, physical findings and precipitating factors of AHF. A classification according to the initial clinical presentation was proposed by the European Society of Cardiology.6 In EuroHF II2 acute decompensation of a pre-existing CHF (ADCHF) with signs of pulmonary congestion and low cardiac output was the most frequent form of AHF, occurring in 65% of patients, followed by pulmonary edema (16%), HF and hypertension (11%), cardiogenic shock (4%) and right HF (3%). In about 30% of cases AHF was the first (de novo) manifestation of a previously unknown cardiac disease. Patients with AHF require urgent therapeutic measures to reduce symptoms, improve the hemodynamic disturbancies and prevent further deterioration. Thus, drug choices, dosages and mode of administration may considerably differ from those in CHF where treatment can be adjusted over a longer period.


Therapeutic options in ADCHF

The initial management of AHF depends on the underlying cardiac disease, preceding drug treatment and precipitating factors. If present, hypertension, arrhythmias or acute coronary syndromes have to be treated first as soon as possible. Among the symptomatic measures to improve dyspnea and relieve congestion vasodilators and/or high ceiling diuretics are usually the drugs of initial choice. Nitroglycerine or isosorbide dinitrate iv have been shown to be superior to repeated high doses of furosemide in patients with pulmonary edema.7 One of the disadvantages of nitrates is a loss of efficacy due to tachyphylaxis within the first 24 to 48 hours. A new alternative for vasodilation is nesiritide, a brain natriuretic peptide (BNP) analogon, which has effects comparable to nitroglycerin without reduction of activity during prolonged administration.8 This drug has been widely used in the USA, but there were negative reports concerning a worsening renal function9 and a trend to higher mortality under nesiritide.10

Although the increased risks have been partly refuted by a retrospective analysis11 the final value of nesiritide needs to be evaluated in further trials. If pulmonary congestion does not rapidly respond to drug treatment a noninvasive positive pressure ventilation by a face mask is a well documented effective therapeutic measure in AHF with pulmonary edema.12

One of the controversial issues in ADCHF is the use of inotropic agents. If signs of low cardiac output with peripheral vasoconstriction and oliguria persist despite correction or exclusion of a hypovolemia and patients do not respond to vasodilators and diuretics, an improvement of myocardial contractility might be needed to correct the severe cardiovascular dysfunction. For this reason beta-adrenergic drugs, dobutamine and dopamine, or phosphodiesterase inhibitors, milrinone and enoximone, are often administered. Although these agents produce a symptomatic and hemodynamic improvement, their influences on clinical outcomes are mostly negative. Increased myocardial oxygen requirements and pro-arrhythmia are well known undesired effects which may seriously compromise the utility of inotropic therapy.13?15

A new category of cardio-stimulant drugs with combined positive inotropic and vasodilating effects, the calcium sensitizers, may avoid some of the disadvantages of other inotropic agents and offer a therapeutic alternative in patients with ADCHF. Levosimendan is the best studied calcium sensitizer and is available for routine clinical use in several European countries, as well as in Brasil, Argentina and Mexico. This review will focus on the clinical pharmacology of levosimendan, its dosage, indications and analyze the results of clinical trials.


Clinical pharmacology of levosimendan

The positive inotropic action of levosimendan is due to its binding to troponin C which facilitates the interaction between actin and myosine filaments without changes in intracellular Ca++ ion concentrations.16 In addition, the drug produces peripheral and coronary vasodilation by opening ATP-sensitive potassium channels.17 This dual mechanism of action results in an improved myocardial contractility without relevant changes in oxygen requirements18 and in a reduction of post-ischemic stunning.19,20

The pharmacokinetic and pharmacodynamic properties of levosimendan have been studied in healthy volunteers and patients with heart failure.21,22 Following intravenous administration in different dosages the pharmacokinetics remained linear with an elimination half-life of the unchanged compound of around 1 hour. Complete metabolism with formation of two pharmacologically active products (OR-1896 and OR-1855) is the mechanism of hepatic excretion. These metabolites are eliminated very slowly with half-lives of >80 and >70 hours, respectively. Because their activity is similar to that of levosimendan the pharmacodynamic effects of a 24-hour infusion last up to several days.23 For this reason more prolonged infusions are not recommended. In patients with heart failure and mild to moderate renal dysfunction, pharmacokinetics changed little, but in patients with end-stage renal disease undergoing hemodialysis, an accumulation of the active metabolites could be observed.24 Thus, initial dose reduction (starting with 0.05 ?g/kg/min) is necessary if levosimendan is used in patients with ADCHF and renal dysfunction. There are few data available on the extent of metabolite accumulation in patients with liver disease.25 In 12 cases with alcoholic cirrhosis there was a slight prolongation of metabolite half-lives (+30%), which would again indicate lower initial infusion rates, similar to those in patients with renal failure.

The hemodynamic effects of levosimendan have been evaluated in dose finding studies in patients with CHF.26 After initial iv bolus infusions of 3, 6, 12, 24 or 36 ?g/kg in 10 minutes, followed by 24-hour continuous infusions at rates of 0.05, 0.1, 0.2, 0.4 and 0.6 ?g/kg/min, dose-dependent increases of cardiac output and stroke volume together with a rapid decreases of pulmonary capillary wedge pressure and right atrial pressure were measured. Slight heart rate increases and reductions in mean blood pressure were also seen. Calculated peripheral vascular resistance was linearly reduced with increasing doses. Protocol defined dose limiting events were tachycardia >20% and systolic blood pressure <90 mmHg, mainly in patients receiving higher doses of 0.4 and 0.6 ?g/kg/min. Headaches and nausea also occurred in some cases. Based on this study infusion rates of 0.05 to 0.2 ?g/kg/min were recommended to achieve favorable hemodynamic effects with good tolerance.


Clinical trials with levosimendan

The first randomized, double-blind, multicenter trial (LIDO) compared levosimendan with dobutamine in 203 hospitalized patients with severe low output CHF.27 Inclusion criteria were an ejection fraction <35%, a cardiac index <2.5 L/min/m2 and a pulmonary capillary wedge pressure >15 mmHg. All patients were symptomatic under a treatment with ACE inhibitors, diuretics and digoxin; one third also received a beta-blocker. Levosimendan was infused after a loading dose of 24 ?g/kg/min in 10 minutes at a rate of 0.1 ?g/kg/min for 24 hours and dobutamine without loading at 5 ?g/kg/min. Dosage of both drugs was doubled after 2 hours if the intended hemodynamic improvement, defined as increase of cardiac index by 30% and reduction of pulmonary capillary wedge pressure by 25%, was not achieved. This end-point was reached in 28% of patients with levosimendan compared to only 15% with dobutamine (p < 0.022). In the subgroup of patients under beta-blockade therapeutic targets were obtained in 10 out of 33 under levosimendan versus 3 of 29 cases under dobutamine, respectively. Furthermore, levosimendan also had a beneficial effect on clinical outcomes: at 31 days mortality was lower after levosimendan with 8 deaths (8%) versus 17 (17%) after dobutamine (hazard ratio 0.43 [0.18?1.0], p = 0.049). The prognostic benefit persisted up to 180 days, the median number of days alive and out of hospital being 157 (101?173) in the levosimendan group and 133 (43.5?169) after dobutamine (p = 0.027). The total number of adverse events was comparable in both treatment groups (48 vs 42 events, p 0.88), but more arrhythmias14 occurred under dobutamine than under levosimendan,4 p < 0.023, while hypotension was observed in 9 patients under levosimendan compared to 4 under dobutamine (p = 0.252). Thus, there was an overall advantage of levosimendan in this trial.

The second randomized clinical trial (RUSSLAN) compared levosimendan, infused for 6 hours in 4 different doses, with placebo in 504 patients with clinical and radiological signs of left ventricular failure following an acute myocardial infarction.28 The primary aim was to test the tolerability of levosimendan with the end-points hypotension and myocardial ischemia. Secondary end-points included all cause mortality and worsening HF. At doses of 0.1 to 0.2 ?g/kg/min levosimendan did not increase the incidence of hypotension or ischemia and reduced the combined risk of death and worsening HF during the first 24 hours (4% versus 8.8% in the placebo group, p = 0.044). There was, however, a non-significant trend for a higher risk of hypotension and/or ischemia at the highest dose (0.4 ?g/kg/min) of levosimendan. Mortality at 14 days was 19.6% after placebo compared to 10.0% to 13.1% (average 11.7%) in the four subgroups receiving levosimendan (p = 0.031), but after 180 days the differences were no more statistically significant.

More recently, two larger randomized, double-blind trials were conducted in the USA and in Europe. In REVIVE II, 24-hour infusions of levosimendan were compared with placebo in 600 patients with ADCHF.29 The primary ?composite? end-point was a measure of the clinical course, based on subjective and objective symptom assessments over 5 days. Levosimendan was given after an initial loading of 12 ?g/kg in 10 minutes followed by a uniform infusion rate of 0.2 ?g/kg/min for 24 hours. Co-administration of iv diuretics and vasodilators was allowed without hemodynamic monitoring. At 5 days 33% more patients improved and 26% fewer worsened after levosimendan than placebo (p = 0.015). This positive clinical outcome was, however, partially neutralized by a high incidence of hypotension (50.2 vs 36.4%, p < 0.01) and more frequent atrial fibrillation (8.5 vs 2.0%) under levosimendan and placebo, respectively. There was also a non-significant negative trend for higher mortality at 14 and 31 days following levosimendan. The SURVIVE trial30 compared levosimendan with dobutamine in 1327 patients with acute heart failure judged to require inotropic support. Again, levosimendan was given in a uniform high dosage at 0.2 ?g/kg/min to all patients for 24 hours; the average dose of dobutamine was 6 ?g/kg/min. Patients were hospitalized at intensive care units but not invasively monitored. Also in this trial iv diuretics and concomitant vasodilators were allowed. The primary end-point was survival at 180 days. At the end of follow up there were 173 deaths (26%) in the levosimendan group as compared to 185 (28%) on placebo (p = 0.4). However, a subgroup analysis at 31 days showed a survival advantage of levosimendan in patients with a prior history of heart failure. Also plasma BNP levels decreased significantly more at 24 hours and at 3 to 5 days after levosimendan than after dobutamine. The rates of serious adverse events were not different in the two treatments groups, but there were more hypotensions and higher heart rate increases under levosimendan, while patients were less likely to experience worsening cardiac failure than under dobutamine.

Following the presentation of REVIVE II and SURVIVE doubts were voiced regarding the utility of levosimendan in the treatment of AHF.31 For this reason it is important to analyze the basic differences between the initially positive and the more recent partly contradictory trial results and try to explain the variable outcomes. In the LIDO trial all patients were hemodynamically monitored and had initial capillary wedge pressures of 15 mmHg or more (mean 25 ? 8 mmHg), as well as a cardiac index <2.5 L/kg/m2. Thus, they all belonged to a well defined category of ADCHF patients; cases with signs of active myocardial ischemia or acute arrhythmias were excluded. Co-administration of iv diuretics or vasodilators was not allowed. In contrast, both in REVIVE and SURVIVE, simultaneous treatment with the above drugs, often at high doses, was permitted without invasive monitoring. Hence, a drug-induced hypovolemia could not be excluded and was probably present in many cases. The high incidence of hypotension (36.4%) even under placebo in REVIVE II would fit this assumption. Administering levosimendan, with its marked vasodilating effect at high and uniform doses, especially to heavily pre-treated patients, can be expected to result in marked drops in blood pressure and also lead to cardiac arrhythmias in patients with an underlying coronary artery disease which in SURVIVE was present in over 60%. Hypokalemia due to intensive diuretic administration was an other potentially negative factor. Thus, in retrospect the design in both trials can be questioned. The main lesson from these two recent trials is that a high initial infusion rate of levosimendan has to be avoided and pre-existing hypovolemia be excluded before starting this treatment. In critical cases, especially with systolic blood pressure values < 100 mmHg, infusion should be initiated without loading at only 0.05 ?g/kg/min under close observation to avoid severe hypotension.


Levosimendan in routine clinical practice

There are also observational studies available documenting the practical experience with levosimendan in everyday practice. A Brazilian cohort32 including 182 high risk patients with decompensated HF received open label levosimendan infusions added to a baseline treatment with diuretics, ACE inhibitors/angiotensin receptor antagonists and beta-blockers. In 39% inotropic agents were already used before without success. Out of the 182 patients 139 (76.4%) responded, defined by reduction of dyspnea and of auscultatory signs of pulmonary congestion and could be discharged from hospital. Treatment success was even better (83.3%) in patients on beta-blockers (21%). Levosimendan was said to be well tolerated; no severe hypotension or an increase in cardiac arrhythmias occurred. Nevertheless, 54 patients had some adverse events which resolved spontaneously or after dose reduction. Mortality rate during hospitalization was 14.8% in patients responding to levosimendan compared to 62.8% in non-responders. A similar positive practical experience was reported from Portugal.33 In an open, prospective, multicenter study in 129 hospitalized patients with systolic HF and signs of decompensation, a 24-hour infusion of levosimendan at a dose of 0.05 to 0.1 ?g/kg/min was given as a first line inotropic therapy. During an observation period of 5 days a well defined clinical improvement (reduction of NYHA class and increased diuresis with reduction of serum creatinine) without additional inotropes and no adverse events was obtained in 80%. These observational data indicate that levosimendan can be safely and successfully used under everyday routine clinical conditions.


Levosimendan and renal function

An important advantage of levosimendan is its potential to improve renal function in patients with ADCHF. A significant reduction of serum creatinine was reported already in the initial clinical trial.27 Subsequently, two studies were specially conducted to evaluate the effects of levosimendan on serum creatinine and glomerular filtration rate (GFR). In 40 patients with advanced CHF and increased serum creatine values (1.92 ? 0.13 mg/dL), a 24-hour infusion at a dose of 0.1 ? g/kg/min compared to a control group without inotropic support, but otherwise identical treatment, showed a reduction of serum creatinine by ?0.32 ? 0.28 mg/dL and ?0.01 ? 0.13 mg/dL, respectively.34 After 3 months creatinine clearance was still improved from the initial value of 43.7 ? 2.9 mL/min to 53.6 ? 8.6 mL/min, whereas in the control group GFR did not change. In another study levosimendan was compared with dobutamine, both infused for 24 hours, in 88 consecutive patients with ADCHF.35 Within 24 hours GFR increased by 15.3% under levosimendan versus ?1.33% under dobutamine. GFR values improved further after 72 hours.


Effects of levosimendan on surrogate end-points in HF

Levosimendan was also shown in smaller comparative trials to have potentially beneficial effects not only on neurohormones, but also on inflammatory cytokines and apoptosis mediators in HF. Moertl et al36 observed a BNP reduction by 28% at 24 hours and by 22% at 48 hours following 24 hours levosimendan infusion in patients with decompensated HF, but these effects disappeared after 1 week. Parissis et al37 reported a significant BNP reduction together with further reduction of interleukin-6 (IL-6). In their patients there was also an improvement of left ventricular diastolic function as judged by echocardiographic techniques. Trikas et al38 equally found significant decreases of serum IL-6, TNF-alfa as well as of the apoptosis marker soluble FAS (sFAS). Such surrogate effects could have positive long-term therapeutic influences for levosimendan in addition to its cardio-stimulatory activity, but convincing clinical data in this respect are still lacking.


Emerging indications and treatments

There are also some new indications for levosimendan treatment, such as repetitive administration in patients with advanced HF,39,40 post-operative myocardial dysfunction following cardiac surgery,41 or right ventricular failure.42 These interesting applications require further larger trials to confirm the therapeutic utility of levosimendan.

The recently developed new inotropic and lusitropic agent, istaroxime, which has similar hemodynamic effects and also does not seem to increase myocardial oxygen requirements,43 might become a potential alternative to levosimendan in patients with HF, but the clinical data are still limited.


Conclusions
Current indications and dosage recommendations for levosimendan

Levosimendan represents a new and valuable option for the treatment of properly selected and monitored patients with decompensated heart failure needing inotropic support to prevent further deterioration. The best documented indication for levosimendan is the treatment of patients with ADCHF presenting with high filling pressures, signs of congestion and reduced cardiac output with peripheral vasoconstriction. The combined inodilating effects of levosimendan rapidly relieve pulmonary congestion and improve organ perfusion, including renal blood flow and GFR. However, before starting a levosimendan infusion it is essential to exclude and correct a hypovolemia due to preceding high dose iv diuretics or vasodilators, otherwise an arterial hypotension may occur. Low serum potassium should also be corrected to avoid proarrhythmic effects.

Based on clinical experience in countries in which use is widespread, a loading dose of levosimendan can be omitted in many patients, especially if the initial systolic blood pressure is ?100 mmHg. In view of the short (1 hour) half-life of unchanged levosimendan a near maximum effect of a given infusion rate will be reached within 4 hours without loading. A starting infusion rate of 0.05 ?g/kg/min is usually safe even in critical patients. The dose can be increased to 0.1 ?g/kg/min after 1 to 2 hours if the drug is well tolerated; 0.2 ?g/kg/min might be needed in some patients not adequately responding. The standard duration of infusion is 24 hours, but in some situations, such as intermittent ambulatory administration, a 6- to 8-hour infusion may be more suitable. A prolonged infusion is not recommended, since the slowly formed active metabolites maintain the hemodynamic effects for several days and longer treatments lead to drug accumulation with tachycardia and hypotension.42

The best efficacy can be expected in patients pre-treated with beta-blockers which, in contrast to beta-adrenergic drugs, do not reduce the actions of levosimendan. In patients not yet under beta-blockers these drugs can be safely introduced and uptitrated under protection with levosimendan even after an episode of acute decompensation.


Notes

Disclosures

The author has received lecture fees from, and consulted for, Abbott Laboratories.

References
1. Rudiger A,Harjola VP,M?ller A,et al. Acute heart failure: clinical presentation, one-year mortality and prognostic factorsEur J Heart FailYear: 2004766267015921809
2. Nieminen MS,Brutsaert D,Dickstein K,et al. EuroHeart Failure Survey II: a survey on hospitalised acute heart failure patients: description of populationEur Heart JYear: 2006272725273617000631
3. Tavazzi L,Maggioni A,Lucci D,et al. Nationwide survey on acute heart failure in cardiology ward services in ItalyEur Heart JYear: 2006271207121516603579
4. Siirel?-Waris K,Lassus J,Melin J,Peuhkurinen K,Nieminen MS,Harjola VP. Characteristics, outcomes, and predictors of 1-year mortality in patients hospitalised for acute heart failureEur Heart JYear: 2006273011301717127708
5. Adams KF,Fonarow GC,Emermann CL,et al. Characteristics and outcome of patients hospitalised for heart failure in the United States: rationale, design and preliminary observations from the first 100,000 cases in the Acute Decompensated Heart Failure National Registry (ADHERE)Am Heart JYear: 200514920921615846257
6. The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure of the European Society of CardiologyESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2008Eur Heart JYear: 2008292388244218799522
7. Cotter G,Metzkor E,Kaluski E,et al. Randomised trial of high-dose isosorbide dinitrate plus low-dose furosemide versus high-dose furosemide plus low-dose isosorbide dinitrate in severe pulmonary oedemaLancetYear: 19983513893939482291
8. The VMAC investigatorsIntravenous nesiritde vs nitroglycerine for the treatment of decompensated heart failureJAMAYear: 20022871531154011911755
9. Sackner-Bernstein JD,Skopicki HA,Aaronson KD. Risk of worsening renal function with nesiritide in patients with acutely decompensated heart failureCirculationYear: 20051111487149115781736
10. Sackner-Bernstein JD,Kowalski M,Fox M,Aaronson K. Short term risk of death after treatment with nesiritide for decompensated heart failure. A pooled analysis of randomised controlled trialsJAMAYear: 20052931900190515840865
11. Arora S,Clarke K,Srinivasan V,Gradman A. Effect of nesiritide on renal function in patients admitted for decompensated heart failureQJMYear: 200710069970617971392
12. Peter JV,Moran JL,Philips-Hughes J,Graham P,Bersten AD. Effect of non-invasive positive pressure ventilation (NIPPV) on mortality in patients with acute cardiogenic pulmonary oedema: a meta-analysisLancetYear: 20063671155116216616558
13. O?Connor CM,Gattis WS,Uretsky BF,et al. Continuous intravenous dobutatmine is associated with an increased risk of death in patients with advanced heart failure: Insights from the Flolan International Randomised Survival Trial (FIRST)Am Heart JYear: 1999138788610385768
14. Thackray S,Easthaugh J,Fremantle N,et al. The effectiveness and relative effectiveness of intravenous inotropic drugs acting through the adrenergic pathway in patients with heart failure ? meta-regression analysisEur J Heart FailYear: 2002451552912167393
15. Cuffe MS,Califf MR,Adams KF,et al. Short-term intravenous milrinone for acute exacerbation of chronic heart failureJAMAYear: 20022871541154711911756
16. Haikala H,Kaivola J,Nissinen E,et al. Cardiac troponin C as a target protein for a novel calcium sensitizing drug, levosimendanJ Mol Cell CardiolYear: 199527185918668523447
17. Yokoshiki H,Kutsube Y,Sunagawa M,et al. The novel calcium sensitizer levosimendan activates the ATP-sensitive K+ channel in rat ventricular cellsJ Pharmacol Exp TherYear: 19972833753839336346
18. Ukkonen H,Saraste M,Akkila J. Myocardial efficiency during levosimendan infusion in congestive heart failureClin Pharmacol TherYear: 20006852253111103755
19. Jamali IN,Kersten JR,Pagel PS,et al. Intracoronary levosimendan enhances contractile function of stunned myocardiumAnaesth AnalgYear: 1997852329
20. Sonntag S,Sudberg S,Lehtonen LH,Kleber FX. The calcium sensitizer levosimendan improves the function of stunned myocardium after percutaneous transluminal coronary angioplasty in acute myocardial ischemiaJ Am Coll CardiolYear: 2004432177218215193677
21. Lilleberg J,Sundberg S,H?yh? M,et al. Haemodynamic dose-efficacy of levosimendan in healthy volunteersEur J Clin PharmacolYear: 1994472672747867680
22. Kivikko M,Antila S,Eha J,Lehtonen L,Pentik?inen PJ. Pharmacodynamics and safety of a new calcium sensitzer, levosimendan, and its metabolites during an extended infusion in patients with severe heart failureJ Clin PharmacolYear: 200242435111808823
23. Lilleberg J,Laine M,Palkama T,Kivikko M,Pohjanjousi P,Kupari M. Duration of the haemodynamic action of a 24-h infusion of levosimendan in patients with congestive heart failureEur J Heart FailYear: 20079758216829185
24. Puttonen J,Kantele S,Kivikko M,et al. Effect of severe renal failure and haemodialysis on the pharmacokinetics of levosimendan and its metabolitesClin PharmacokinetYear: 20074623524617328582
25. Puttonen J,Kantele S,Ruck A,et al. Pharmacokinetics of intravenous levosimendan and its metabolites in subjects with hepatic impairmentJ Clin PharmacolYear: 20084844545418303124
26. Nieminen MS,Akkila J,Hasenfuss G,et al. Haemodynamic and neurohumoral effects of continuous infusion of levosimendan in patients with congestive heart failureJ Am Coll CardiolYear: 2000361903191211092663
27. Follath F,Cleland JGF,Just H,et al. Efficacy and safety of intravenous levosimendan compared with dobutamine in severe low-output heart failure (the LIDO study): a randomised double-blind trialLancetYear: 200236019620212133653
28. Moiseyev VS,Poder P,Andrejevs N,et al. Safety and efficacy of a novel calcium sensitizer, levosimendan, in patients with left ventricular failure due to an acute myocardial infarction. A randomised, placebo controlled, double blind study (RUSSLAN)Eur Heart JYear: 2002231422143212208222
29. Packer M. REVIVE II: Multicenter placebo controlled trial of levosimendan on clinical status in acutely decompensated heart failure. American Heart Association Scientific Sessions 2005, November 13?16, Dallas, Texas. Late breaking clinical trials IICirculationYear: 20051123363
30. Mebazaa A,Nieminen MS,Packer M,et al. Levosimndan vs dobutamine for patients with acute decompensated heart failure. The SURVIVE randomised trialJAMAYear: 20072971883189117473298
31. Petersen JW,Felker GM. Inotropes in the management of acute heart failureCrit Care MedYear: 2008361 SupplS106S11118158469
32. Bocchi AE,Vilas-Boas F,Moreira MC,et al. Levosimendan in decompensated heart failure patients: efficacy in a Brasilian Cohort. Results of the BELIEF studyArq Bras CardiolYear: 20089018219018392398
33. Silva-Cardoso J,Ferriera J,Prazeredes de S? E,et al. Levosimendan in daily intensive care practice- the experience of 15 centres. Background, methods and organisation of the PORTLAND studyRev Port CardiolYear: 2004231431144315693696
34. Zemljic G,Bunc M,Yazdanbakhsh AP,Vrtovec B. Levosimendan improves renal function in patients with advanced heart failure awaiting cardiac transplantationJ Card FailYear: 20071341742117675054
35. Yilmaz MB,Yalta K,Yontar C,et al. Levosimendan improves renal function in patients with acute decompensated heart failure: comparison with dobutamineCardiovasc Drugs TherYear: 200721231435
36. Moertl D,Berger R,Huelsmann B,et al. Short-term effects of levosimendan and prostaglandin E1 on hemodynamic parameters and B-type natriuretic peptide levels in patients with decompensated chronic heart failureEur J Heart FailYear: 200571156116316084762
37. Parissis JT,Panou F,Farmakis D,et al. Effects of levosimendan on markers of left ventricular diastolic function and neurohumoral activation in patients with advanced heart failureAm J CardiolYear: 20059642342616054474
38. Trikas A,Antoniades C,Latsios G,et al. Log-term effects of levosimendan infusion on inflammatory processes and sFAS in patients with severe heart failureEur J Heart FailYear: 2006880480916713737
39. Berger R,Moertl D,Huelsmann M,et al. Levosimendan and prostaglandin E1 for uptitration of betablockade in patients with advanced chronic heart failureEur J Heart FailYear: 2007920220816859992
40. Nanas JN,Papazouglu PP,Tsagalou EP,et al. Efficacy and safety of intermittent, long-term, concomitant dobutamine and levosimendan infusions in severe heart failure refractory to dobutamine aloneAm J CardiolYear: 20059576877115757608
41. De Hert SG,Losomradee S,Cromheecke S,Van der Linden PJ. The effects of levosimendan in cardiac surgery patiens with poor left ventricular functionAnaesth AnalgYear: 2007104766773
42. Poelzl G,Zwick RH,Grander W,et al. Safety and effectiveness of levosimndan in patients with predominant right heart failureHerzYear: 20083336837318773157
43. Georghiade M,Blair JEA,Filippatos GS,et al. Hemodynamic, echocardiographic, and neurohumoral effects of istaroxime, a novel intravenous inotropic and lusitropic agentJ Am Coll CardiolYear: 2008512276228518534276

Article Categories:
  • Review

Keywords: acute heart failure, inotropic agents, calcium sensitizers, levosimendan.

Previous Document:  Analysis of HSP90-related folds with MED-SuMo classification approach.
Next Document:  Troglitazone reverses the multiple drug resistance phenotype in cancer cells.